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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027327Generated: October 26, 2026

Benzocaine → Ethyl 4-[(1-oxoallyl)amino]benzoate

https://huagongshe.com/reaction/1027327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzocaineHCID 2337—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-[(1-oxoallyl)amino]benzoateHCID 8461876.1%

Reaction Steps

To a solution of acryloyl chloride (1.08 mL, 13.32 mmol) in dry dichloromethane (10 mL) was slowly added dropwise, via addition funnel, a solution of 4-aminobenzoic acid ethyl ester (2.0 g, 12.11 mmol) and triethylamine (1.86 mL, 13.32 mmol) in dry dichloromethane (5 mL) over about 30 minutes. The reaction was stirred at room temperature for 16 hours. The solution was then partitioned between dichloromethane and water in a separatory funnel. The organic layer was washed with 2 N HCl, dried with sodium sulfate, and concentrated in vacuo to dryness. The resulting residue was triturated with hexane, and vacuum filtered to yield 2.02 g (76%) of 4-acryloylaminobenzoic acid ethyl ester as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08734818B2
Source datasetuspto-grants-2014_05
ORD IDord-ffc35e68ed79484bb79c18218abbad1d
Source noteuspto-grants-2014_05